نتایج جستجو برای: multiple hereditary

تعداد نتایج: 831640  

Journal: :Annals of Physical and Rehabilitation Medicine 2012

Journal: :Proceedings of the Royal Society of Medicine 1935

Journal: :Ankara Üniversitesi Tıp Fakültesi Mecmuası 2006

2011
Sadhanna Badeloe Jorge Frank

Alias Multiple cutaneous and uterine leiomyomatosis (MCUL) Hereditary leiomyomatosis and renal cell cancer (HLRCC) Note Multiple cutaneous leiomyomatosis (MCUL) is characterized by multiple leiomyomas of the skin and uterus. When associated with renal cell cancer, this syndrome is referred to as hereditary leiomyomatosis and renal cell cancer (HLRCC). Inheritance Autosomal dominant with incompl...

اولیاء, محمدباقر, بهرامی احمدی, امیر, شاکری, جواد, علیشیری, غلامحسین ,

Familial Mediterranean fever (FMF) is a hereditary condition which is characterized by recurrent episodes of fever and abdominal pain. On the other hand, Behcet`s disease (BD) is an immune mediated condition typified by recurrent oral aphthous lesions, inflammatory eye disease and multiple organ involvement. Association of these two conditions is rare. We present a pair of twins with FMF and B...

2008
Matthew M. Robbins Scott Kuo Robert Epstein

A 38-year-old man with a known history of hereditary multiple exostoses and no history of trauma presented with a painful right femur mass. While the clinical presentation was concerning for malignant degeneration or a large overlying bursitis, the radiologic evaluation demonstrated a large fractured pedunculated osteochondroma with a thick cartilage cap and underlying bone marrow edema. Trauma...

Journal: :iranian journal of public health 0
hosein dalili family health institute, breastfeeding research center, tehran university of medical sciences, tehran, iran. elahe amini family health institute, maternal- fetal& neonatal research center, tehran university of medical sciences, tehran, iran. parvin akbari asbagh dept. of pediatric, school of medicine, tehran university of medical sciences, tehran, iran. tahereh esmaeilnia shrivany family health institute, breastfeeding research center, tehran university of medical sciences, tehran, iran. nikoo niknafs family health institute, maternal- fetal& neonatal research center, tehran university of medical sciences, tehran, iran. fatemeh nayyeri family health institute, maternal- fetal& neonatal research center, tehran university of medical sciences, tehran, iran.

tuberous sclerosis complex (tsc) is an autosomal-dominant hereditary disorder. this syndrome is characterized by tumor-like malformations in several organs, as well as the heart. this report summarizes a case of tsc in a premature infant, born at 34 weeks' gestation with ascites. after birth, multiple cardiac mass, subependymal cysts and hypopigmented macules were detected. to our knowledge, th...

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